• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

人类肠道微生物组和血清代谢组的整合揭示了参与调节骨密度的新生物学因素。

Integration of the Human Gut Microbiome and Serum Metabolome Reveals Novel Biological Factors Involved in the Regulation of Bone Mineral Density.

机构信息

Tulane Center of Biomedical Informatics and Genomics, Deming Department of Medicine, Tulane University School of Medicine, Tulane University, New Orleans, LA, United States.

Department of Endocrinology and Metabolism, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China.

出版信息

Front Cell Infect Microbiol. 2022 Mar 16;12:853499. doi: 10.3389/fcimb.2022.853499. eCollection 2022.

DOI:10.3389/fcimb.2022.853499
PMID:35372129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8966780/
Abstract

While the gut microbiome has been reported to play a role in bone metabolism, the individual species and underlying functional mechanisms have not yet been characterized. We conducted a systematic multi-omics analysis using paired metagenomic and untargeted serum metabolomic profiles from a large sample of 499 peri- and early post-menopausal women to identify the potential crosstalk between these biological factors which may be involved in the regulation of bone mineral density (BMD). Single omics association analyses identified 22 bacteria species and 17 serum metabolites for putative association with BMD. Among the identified bacteria, and were negatively associated, while were positively associated. Several of the identified serum metabolites including 3-phenylpropanoic acid, mainly derived from dietary polyphenols, and glycolithocholic acid, a secondary bile acid, are metabolic byproducts of the microbiota. We further conducted a supervised integrative feature selection with respect to BMD and constructed the inter-omics partial correlation network. Although still requiring replication and validation in future studies, the findings from this exploratory analysis provide novel insights into the interrelationships between the gut microbiome and serum metabolome that may potentially play a role in skeletal remodeling processes.

摘要

虽然肠道微生物群已被报道在骨骼代谢中发挥作用,但个体物种和潜在的功能机制尚未得到阐明。我们使用来自 499 名绝经前和早期绝经后女性的配对宏基因组和非靶向血清代谢组学图谱进行了系统的多组学分析,以确定这些生物因素之间可能涉及骨密度 (BMD) 调节的潜在串扰。单组学关联分析确定了 22 种细菌物种和 17 种与 BMD 可能相关的血清代谢物。在鉴定出的细菌中, 和 呈负相关,而 呈正相关。鉴定出的几种血清代谢物,包括主要来源于膳食多酚的 3-苯丙酸和次级胆汁酸甘氨胆酸,是微生物群的代谢副产物。我们进一步针对 BMD 进行了有监督的综合特征选择,并构建了组间部分相关网络。尽管这些发现仍需要在未来的研究中进行复制和验证,但这项探索性分析提供了肠道微生物组和血清代谢组之间相互关系的新见解,这些相互关系可能在骨骼重塑过程中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81eb/8966780/dd2b434c77de/fcimb-12-853499-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81eb/8966780/012289dc3803/fcimb-12-853499-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81eb/8966780/d1aa88368a73/fcimb-12-853499-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81eb/8966780/832e38657a90/fcimb-12-853499-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81eb/8966780/f7b92c7b8aec/fcimb-12-853499-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81eb/8966780/dd2b434c77de/fcimb-12-853499-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81eb/8966780/012289dc3803/fcimb-12-853499-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81eb/8966780/d1aa88368a73/fcimb-12-853499-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81eb/8966780/832e38657a90/fcimb-12-853499-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81eb/8966780/f7b92c7b8aec/fcimb-12-853499-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81eb/8966780/dd2b434c77de/fcimb-12-853499-g005.jpg

相似文献

1
Integration of the Human Gut Microbiome and Serum Metabolome Reveals Novel Biological Factors Involved in the Regulation of Bone Mineral Density.人类肠道微生物组和血清代谢组的整合揭示了参与调节骨密度的新生物学因素。
Front Cell Infect Microbiol. 2022 Mar 16;12:853499. doi: 10.3389/fcimb.2022.853499. eCollection 2022.
2
Characteristics of the gut microbiota and serum metabolites in postmenopausal women with reduced bone mineral density.绝经后低骨密度妇女的肠道微生物群特征和血清代谢产物。
Front Cell Infect Microbiol. 2024 Jun 7;14:1367325. doi: 10.3389/fcimb.2024.1367325. eCollection 2024.
3
Machine learning-causal inference based on multi-omics data reveals the association of altered gut bacteria and bile acid metabolism with neonatal jaundice.基于多组学数据的机器学习-因果推断揭示了肠道细菌和胆汁酸代谢改变与新生儿黄疸的关联。
Gut Microbes. 2024 Jan-Dec;16(1):2388805. doi: 10.1080/19490976.2024.2388805. Epub 2024 Aug 21.
4
Alterations of host-gut microbiome interactions in multiple sclerosis.多发性硬化症中宿主-肠道微生物组相互作用的改变。
EBioMedicine. 2022 Feb;76:103798. doi: 10.1016/j.ebiom.2021.103798. Epub 2022 Jan 27.
5
Pivotal interplays between fecal metabolome and gut microbiome reveal functional signatures in cerebral ischemic stroke.粪便代谢组和肠道微生物组之间的关键相互作用揭示了脑缺血性中风的功能特征。
J Transl Med. 2022 Oct 8;20(1):459. doi: 10.1186/s12967-022-03669-0.
6
Network of Interactions Between Gut Microbiome, Host Biomarkers, and Urine Metabolome in Carotid Atherosclerosis.肠道微生物组、宿主生物标志物和颈动脉粥样硬化尿液代谢组之间的相互作用网络。
Front Cell Infect Microbiol. 2021 Oct 7;11:708088. doi: 10.3389/fcimb.2021.708088. eCollection 2021.
7
Gut microbiome and metabolome to discover pathogenic bacteria and probiotics in ankylosing spondylitis.研究肠微生物组和代谢组,以发现强直性脊柱炎中的致病菌和益生菌。
Front Immunol. 2024 Apr 22;15:1369116. doi: 10.3389/fimmu.2024.1369116. eCollection 2024.
8
Impact of Dietary Resistant Starch on the Human Gut Microbiome, Metaproteome, and Metabolome.膳食抗性淀粉对人类肠道微生物组、宏蛋白质组和代谢组的影响。
mBio. 2017 Oct 17;8(5):e01343-17. doi: 10.1128/mBio.01343-17.
9
The unique composition of Indian gut microbiome, gene catalogue, and associated fecal metabolome deciphered using multi-omics approaches.利用多组学方法解析了印度肠道微生物群的独特组成、基因目录及相关粪便代谢组。
Gigascience. 2019 Mar 1;8(3). doi: 10.1093/gigascience/giz004.
10
Age-related alterations in metabolome and microbiome provide insights in dietary transition in giant pandas.代谢组学和微生物组学的年龄相关性改变为大熊猫的饮食转变提供了新的见解。
mSystems. 2023 Jun 29;8(3):e0025223. doi: 10.1128/msystems.00252-23. Epub 2023 Jun 5.

引用本文的文献

1
Gut microbiota changes in postmenopausal women with low bone density linked to serum amino acid metabolism.骨密度低的绝经后女性肠道微生物群的变化与血清氨基酸代谢有关。
Front Cell Infect Microbiol. 2025 Jul 9;15:1627519. doi: 10.3389/fcimb.2025.1627519. eCollection 2025.
2
Gut microbiome dysbiosis accelerates osteoarthritis progression by inducing IFP-SM inflammation in "double-hit" mice.肠道微生物群失调通过在“双打击”小鼠中诱导IFP-SM炎症加速骨关节炎进展。
Arthritis Res Ther. 2025 Jul 7;27(1):137. doi: 10.1186/s13075-025-03602-y.
3
Deciphering the gut microbiome's metabolic code: pathways to bone health and novel therapeutic avenues.

本文引用的文献

1
Gut microbiota impacts bone via Bacteroides vulgatus-valeric acid-related pathways.肠道微生物群通过脆弱拟杆菌-戊酸相关途径影响骨骼。
Nat Commun. 2023 Oct 27;14(1):6853. doi: 10.1038/s41467-023-42005-y.
2
Identification and Functional Characterization of Metabolites for Bone Mass in Peri- and Postmenopausal Chinese Women.围绝经期和绝经后中国女性骨量代谢产物的鉴定与功能特征分析
J Clin Endocrinol Metab. 2021 Jul 13;106(8):e3159-e3177. doi: 10.1210/clinem/dgab146.
3
DIAMOND+MEGAN: Fast and Easy Taxonomic and Functional Analysis of Short and Long Microbiome Sequences.
解读肠道微生物群的代谢密码:通往骨骼健康的途径和新的治疗方法。
Front Endocrinol (Lausanne). 2025 May 22;16:1553655. doi: 10.3389/fendo.2025.1553655. eCollection 2025.
4
Comprehensive Analysis of the Role of Metabolic Features in Osteoporosis: A Multi-Omics Analysis.代谢特征在骨质疏松症中的作用综合分析:多组学分析
Int J Gen Med. 2025 May 26;18:2727-2739. doi: 10.2147/IJGM.S515717. eCollection 2025.
5
Melatonin: A Potential Therapy for Osteoporosis With Insights Into Molecular Mechanisms.褪黑素:对骨质疏松症的一种潜在治疗方法及分子机制洞察
J Pineal Res. 2025 Jul;77(4):e70062. doi: 10.1111/jpi.70062.
6
[Moxibustion Inhibits Postmenopausal Bone Loss by Regulating the Metabolism of Gut Microbiota-Related Serotonin].[艾灸通过调节肠道微生物群相关血清素的代谢抑制绝经后骨质流失]
Sichuan Da Xue Xue Bao Yi Xue Ban. 2025 Jan 20;56(1):129-136. doi: 10.12182/20250160604.
7
Mechanisms of gut homeostasis regulating Th17/Treg cell balance in PMOP.绝经后骨质疏松症中肠道稳态调节Th17/Treg细胞平衡的机制
Front Immunol. 2024 Dec 13;15:1497311. doi: 10.3389/fimmu.2024.1497311. eCollection 2024.
8
Gut microbiome and bone health: update on mechanisms, clinical correlations, and possible treatment strategies.肠道微生物群与骨骼健康:机制、临床关联及潜在治疗策略的最新进展
Osteoporos Int. 2025 Feb;36(2):167-191. doi: 10.1007/s00198-024-07320-0. Epub 2024 Dec 7.
9
Associations between gut microbiota and incident fractures in the FINRISK cohort.肠道微生物群与 FINRISK 队列中骨折事件的相关性。
NPJ Biofilms Microbiomes. 2024 Aug 14;10(1):69. doi: 10.1038/s41522-024-00530-8.
10
Gut microbiota alterations in postmenopausal women with osteoporosis and osteopenia from Shanghai, China.中国上海绝经后骨质疏松症和低骨量妇女的肠道菌群改变。
PeerJ. 2024 May 31;12:e17416. doi: 10.7717/peerj.17416. eCollection 2024.
DIAMOND+MEGAN:快速便捷的短长微生物组序列分类学和功能分析。
Curr Protoc. 2021 Mar;1(3):e59. doi: 10.1002/cpz1.59.
4
Effects of Rare Microbiome Taxa Filtering on Statistical Analysis.稀有微生物群落分类过滤对统计分析的影响。
Front Microbiol. 2021 Jan 12;11:607325. doi: 10.3389/fmicb.2020.607325. eCollection 2020.
5
A Comparative Evaluation of Tools to Predict Metabolite Profiles From Microbiome Sequencing Data.从微生物组测序数据预测代谢物谱的工具的比较评估
Front Microbiol. 2020 Dec 4;11:595910. doi: 10.3389/fmicb.2020.595910. eCollection 2020.
6
Short chain fatty acids in human gut and metabolic health.肠道内的短链脂肪酸与代谢健康。
Benef Microbes. 2020 Sep 1;11(5):411-455. doi: 10.3920/BM2020.0057. Epub 2020 Aug 31.
7
Gut Microbiome Reveals Specific Dysbiosis in Primary Osteoporosis.肠道微生物组揭示原发性骨质疏松症中的特定失调。
Front Cell Infect Microbiol. 2020 Apr 21;10:160. doi: 10.3389/fcimb.2020.00160. eCollection 2020.
8
The Microbiota-Gut-Brain Axis.肠道微生物群-肠-脑轴。
Physiol Rev. 2019 Oct 1;99(4):1877-2013. doi: 10.1152/physrev.00018.2018.
9
Gut microbiota alterations associated with reduced bone mineral density in older adults.老年人骨密度降低与肠道微生物群改变有关。
Rheumatology (Oxford). 2019 Dec 1;58(12):2295-2304. doi: 10.1093/rheumatology/kez302.
10
Predictive metabolomic profiling of microbial communities using amplicon or metagenomic sequences.基于扩增子或宏基因组序列的微生物群落的预测代谢组学分析。
Nat Commun. 2019 Jul 17;10(1):3136. doi: 10.1038/s41467-019-10927-1.